Cervical Sympathetic Chain Neurilemmoma with Postoperative Horner Syndrome.
- Author:
Jae Gu CHO
1
;
Jong Seok SONG
;
Jeong Su WOO
;
Heung Man LEE
Author Information
1. Department of Otolaryngology-Head and Neck Surgery, Korea University College of Medicine, Seoul, Korea. hmlee91@hotmail.com
- Publication Type:Case Report
- Keywords:
Neurilemmoma;
Sympathetic nervous system;
Horner syndrome
- MeSH:
Adult;
Biopsy;
Biopsy, Fine-Needle;
Carotid Arteries;
Female;
Horner Syndrome*;
Humans;
Jugular Veins;
Miosis;
Neck;
Neurilemmoma*;
Sympathetic Nervous System
- From:Korean Journal of Otolaryngology - Head and Neck Surgery
2004;47(3):279-281
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Neurilemmoma arising from the cervical sympathetic chain is not common. It is most often manifested as a solitary, benign, and slow-growing mass, and its malignant degeneration is rare. Recently, we experienced a case of schwannoma arising from cervical sympathetic chain. A 43-year-old woman presented a left neck mass that was found incidentally. Measuring approximately 3x3 cm, the mass was located medial to the left sternocleidomastoid muscle at the level of the carotid bifurcation. Fine needle aspiration biopsy was performed, but no diagnostic information was given. A computed tomography (CT) scan showed a heterogenous, poorly-demarcated mass in the left poststyloid parapharyngeal space, displacing the carotid artery anteriorly and the internal jugular vein laterally. Tumor was excised via transcervical approach. Postoperatively, the patient exhibited mild miosis with ptosis in the left eye. We report this case with a brief review of literature.
